Canonical Allele Identifier: CA10603246
Gene: GCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280517
ClinVar RCV Id: RCV000334247
dbSNP Id: rs886041708

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54902505C>T , CM000676.2:g.54902505C>T GRCh38
NC_000014.8:g.55369223C>T , CM000676.1:g.55369223C>T GRCh37
NC_000014.7:g.54438973C>T NCBI36
NG_008647.1:g.5320G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395514.5:c.159G>A ENSP00000378890.1:p.Trp53Ter
ENST00000491895.6:c.159G>A ENSP00000419045.2:p.Trp53Ter
ENST00000536224.2:c.159G>A ENSP00000445246.2:p.Trp53Ter
ENST00000543643.6:c.159G>A ENSP00000444011.2:p.Trp53Ter
ENST00000622544.4:c.159G>A ENSP00000477796.1:p.Trp53Ter
NM_000161.2:c.159G>A NP_000152.1:p.Trp53Ter
NM_001024024.1:c.159G>A NP_001019195.1:p.Trp53Ter
NM_001024070.1:c.159G>A NP_001019241.1:p.Trp53Ter
NM_001024071.1:c.159G>A NP_001019242.1:p.Trp53Ter
XM_005267530.1:c.159G>A XP_005267587.1:p.Trp53Ter
XM_011536643.1:c.159G>A XP_011534945.1:p.Trp53Ter
NM_000161.3:c.159G>A MANE Select NP_000152.1:p.Trp53Ter
NM_001024070.2:c.159G>A NP_001019241.1:p.Trp53Ter
NM_001024071.2:c.159G>A NP_001019242.1:p.Trp53Ter
NM_001024024.2:c.159G>A NP_001019195.1:p.Trp53Ter